Tedor Pharma Services has invested in and expanded our flexible GMP facility to provide high-quality, cost-competitive development and manufacturing services for a growing portfolio of small molecule, solid dose products from development to commercialization. Based in Cumberland, RI (an hour south of Boston, MA), we can support IND, NDA, and ANDA regulatory filings, needed tech transfers, as well as manufacture approved products.
Have It Made
with Quality Manufacturing
Our facility seamlessly integrates pilot- and commercial-scale processes and equipment for smooth scale-up and end-to-end solutions. Based in the USA, our facility increases reliability of supply by simplifying tech transfer, offering secure shipping, and we manage raw materials and packaging components inventory to align with our partners’ requirements.
In addition to providing innovative solutions and efficient services, Tedor has a strong regulatory track record and robust quality systems. Our facility is FDA registered and inspected, and we are DEA licensed to manufacture controlled substances schedules II through V. Likewise, our GMP analytical laboratory is licensed to handle substances schedules CI-CV.
Explore Tedor’s Services
Tedor specializes in the development and manufacturing of small-molecule pharmaceuticals. Our services include analytical testing, drug dosage development, clinical supply, testing, labeling, packaging, distribution, and commercial manufacturing. Learn more about each stage of our end-to-end outsourcing solutions:
Our multiple, well-fitted GMP laboratories ensure we meet FDA compliance requirements for characterization, testing, analytical development and quality assurance, from pre-formulation to commercialization.
Clinical Trial Supply Services
Leverage our expertise in clinical trial guidance to support the entire drug development process, including clinical trial dosage form, placebo manufacturing, quality assurance, and clinical supply chain management.
We provide GMP manufacturing of solid dose pharmaceuticals at ranging scales from small-batch to large-scale commercialization with our purpose-built facility and expert staff.
Produce stable, effective drug delivery platforms for active pharmaceutical ingredients (APIs) with our high-quality process development and validation services.
that fits your needs
Tedor’s commitment to quality manufacturing goes well beyond FDA standards. Our pilot-scale equipment encompasses all of your early-stage needs, including coating, drying, processing, milling & granulating, mixing & blending, characterization, and pressing. Get in touch with us today for an exhaustive list of our pilot-scale equipment.
Tedor supports our clients throughout the path to patients with GMP manufacturing of commercialized products. Our manufacturing services are powered by powerful technologies to produce and monitor your small-molecule drug products. We simplify the tech transfer process for our clients, and our integrated facility provides convenient scale-up. Get in touch with us today for an exhaustive list of our commercial-scale equipment.
Tedor provides flexible analytical services combined with comprehensive regulatory support for the highest level of early phase and clinical development. Get in touch with us today for a complete list of our analytical equipment.